Bofill M, Gombert W, Borthwick N J, Akbar A N, McLaughlin J E, Lee C A, Johnson M A, Pinching A J, Janossy G
Department of Clinical Immunology, Royal Free Hospital and School of Medicine, London, United Kingdom.
Am J Pathol. 1995 Jun;146(6):1542-55.
Infection with human immunodeficiency virus 1 causes profound changes in the lymph nodes of infected patients. In particular, large numbers of CD8+CD45RO+ T cells infiltrate both the paracortex and the germinal centers. These cells contained the cytotoxic granule-associated protein TIA-1 but showed no detectable levels of perforin and shared the same characteristics of the expanded, activated, short-lived CD8+ population found during acute viral infections. These cells expressed low levels of Bcl-2 and are likely to be short-lived in vivo as evidenced by the direct observation of CD8+ apoptotic cells in the paracortical areas of the infected nodes. Changes in the paracortical nonlymphoid populations were also seen. There were reactive changes in the blood vessels, and the macrophage population was expanded and activated. Furthermore, apoptotic bodies were seen in the cytoplasm of the activated CD68+RFD-7+RFD-1+ macrophages pointing to the phagocytic capacity of these cells and their role in the clearance of the apoptotic cells from the tissues. These observations suggest that the persistance of CD8+ population in human immunodeficiency virus 1 infection is not a result of the presence of an abnormal CD8+ population but rather a result of an inappropriate over-stimulation of the CD8+ cells.
人类免疫缺陷病毒1感染会使受感染患者的淋巴结发生深刻变化。特别是,大量CD8+CD45RO+ T细胞浸润副皮质区和生发中心。这些细胞含有细胞毒性颗粒相关蛋白TIA-1,但未检测到穿孔素水平,并且与急性病毒感染期间发现的扩增、活化、短命的CD8+细胞群具有相同特征。这些细胞Bcl-2表达水平低,并且从感染淋巴结副皮质区直接观察到CD8+凋亡细胞表明其在体内可能短命。副皮质区非淋巴细胞群也有变化。血管出现反应性改变,巨噬细胞群扩增并活化。此外,在活化的CD68+RFD-7+RFD-1+巨噬细胞的细胞质中可见凋亡小体,表明这些细胞具有吞噬能力及其在清除组织中凋亡细胞方面的作用。这些观察结果表明,人类免疫缺陷病毒1感染中CD8+细胞群的持续存在不是异常CD8+细胞群存在的结果,而是CD8+细胞过度刺激不当的结果。